Founded in 1967, our laboratory performs tests for physicians and hospitals in a wide area. Since the 1980’s, we have been performing analytical and diagnostic testing for the pharmaceutical industry. We have been offering customer-oriented full central laboratory service for phase I-IV clinical studies since the mid-1990’s. In 2014, we began offering cellular analysis and molecular diagnostic studies of samples in the pre-clinical phase according to GLP and conducting quality checks on the manufacture of active ingredients under GMP conditions.
Spranger Laboratories are accredited according to DIN EN ISO 15189 and DIN EN ISO/IEC 17025.